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NON-CONTACT INFRARED THERMOMETER

K131243 Class II Traditional
Decision Date
2013-11-12
Sponsor / Applicant
Shenzhen Jumper Medical Equipment Co., Ltd.

Technical Specification

510(k) Submission ID K131243
Product Code FLL
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2910
Decision Date 2013-11-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NON-CONTACT INFRARED THERMOMETER received FDA 510(k) clearance under submission number K131243, sponsored by Shenzhen Jumper Medical Equipment Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2013-11-12.

Classification & Regulation

This clearance is catalogued under FDA product code FLL and 21 CFR 880.2910, within the General Hospital review panel as a Class II device.